@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP284015.RAchiOuGac377yy7EWYNnWmB9qrygq94Ak9VRQizXy0WM
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP284015.RAchiOuGac377yy7EWYNnWmB9qrygq94Ak9VRQizXy0WM130_head
{
this:
np:hasAssertion
dgn-np:NP284015.RAchiOuGac377yy7EWYNnWmB9qrygq94Ak9VRQizXy0WM130_assertion
;
np:hasProvenance
dgn-np:NP284015.RAchiOuGac377yy7EWYNnWmB9qrygq94Ak9VRQizXy0WM130_provenance
;
np:hasPublicationInfo
dgn-np:NP284015.RAchiOuGac377yy7EWYNnWmB9qrygq94Ak9VRQizXy0WM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP284015.RAchiOuGac377yy7EWYNnWmB9qrygq94Ak9VRQizXy0WM130_assertion
a
np:Assertion
.
dgn-np:NP284015.RAchiOuGac377yy7EWYNnWmB9qrygq94Ak9VRQizXy0WM130_provenance
a
np:Provenance
.
dgn-np:NP284015.RAchiOuGac377yy7EWYNnWmB9qrygq94Ak9VRQizXy0WM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP284015.RAchiOuGac377yy7EWYNnWmB9qrygq94Ak9VRQizXy0WM130_assertion
{
miriam-gene:114609
a
ncit:C16612
.
lld:C0024530
a
ncit:C7057
.
dgn-gda:DGN3a8d68e4d9036deff1f2aaf1d84934a8
sio:SIO_000628
miriam-gene:114609
,
lld:C0024530
;
a
sio:SIO_001121
.
}
dgn-np:NP284015.RAchiOuGac377yy7EWYNnWmB9qrygq94Ak9VRQizXy0WM130_provenance
{
dgn-np:NP284015.RAchiOuGac377yy7EWYNnWmB9qrygq94Ak9VRQizXy0WM130_assertion
dcterms:description
"[A mutation (S180L) in the TLR downstream signal transducer TIRAP has recently been reported to be common in Europeans and Africans and to roughly half the risks of heterogeneous infectious diseases including malaria, tuberculosis, bacteremia, and invasive pneumococal disease in heterozygous mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:19602285
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP284015.RAchiOuGac377yy7EWYNnWmB9qrygq94Ak9VRQizXy0WM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:40+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}